EP2394659B1 - Compositions et procédés pour le diagnostic, le traitement et la prévention des cancers répondant à l'hormone de croissance - Google Patents

Compositions et procédés pour le diagnostic, le traitement et la prévention des cancers répondant à l'hormone de croissance Download PDF

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EP2394659B1
EP2394659B1 EP10184646.7A EP10184646A EP2394659B1 EP 2394659 B1 EP2394659 B1 EP 2394659B1 EP 10184646 A EP10184646 A EP 10184646A EP 2394659 B1 EP2394659 B1 EP 2394659B1
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serum
cells
steroid hormone
cell
growth
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EP2394659A1 (fr
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David A. Sirbasku
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Signe BioPharma Inc
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Claims (15)

  1. Composition de sérum de contrôle négatif comprenant:
    au moins une immunoglobuline sécrétoire choisie dans le groupe constitué de IgA, IgM et IgG sous une forme inactivée par rapport à la capacité d'inhiber la prolifération de cellules sensibles aux hormones stéroïdes en l'absence d'hormones stéroïdes; et
    un plasma sanguin appauvri en hormones stéroïdes ou un sérum sanguin appauvri en hormones stéroïdes.
  2. Composition de sérum de contrôle négatif selon la revendication 1, dans laquelle ladite au moins une immunoglobuline sécrétoire est inactivée en chauffant ledit plasma ou sérum sanguin appauvri en hormones stéroïdes contenant l'inhibiteur à base d'immunoglobuline à environ 50-60°C pendant une période de temps suffisante pour rendre l'inhibiteur inactif par rapport à la capacité d'inhiber la croissance de cellules cancéreuses sensibles aux hormones stéroïdes in vitro.
  3. Composition de sérum de contrôle négatif selon la revendication 2, dans laquelle la période de temps est entre environ 90 minutes et environ 30 h.
  4. Composition de sérum de contrôle négatif selon la revendication 1, dans laquelle ladite au moins une immunoglobuline sécrétoire est inactivée par:
    l'obtention d'un échantillon de sérum frais ou congelé non inactivé thermiquement;
    la réalisation d'une première extraction par charbon actif-dextrane sur l'échantillon à environ 30-37°C pour donner un premier sérum extrait; et
    la réalisation d'une deuxième extraction par charbon actif-dextrane à 30-37°C sur le premier sérum extrait pour donner un sérum appauvri en hormones stéroïdes ayant une activité réversible par des hormones stéroïdes d'inhibition de la croissance de cellules cancéreuses sensibles aux hormones stéroïdes.
  5. Composition de sérum de contrôle négatif selon la revendication 1, dans laquelle ladite au moins une immunoglobuline sécrétoire est inactivée par:
    la réalisation d'une extraction par résine échangeuse d'ions XAD™ d'un sérum frais ou congelé non inactivé thermiquement pour donner un sérum appauvri en hormones stéroïdes ayant une activité réversible par des hormones stéroïdes pour l'inhibition de la croissance de cellules cancéreuses sensibles aux hormones stéroïdes.
  6. Composition de sérum de contrôle négatif selon la revendication 1 pour une utilisation dans un test de prolifération de cellules cancéreuses.
  7. Sérum de contrôle négatif selon la revendication 1, dans lequel ladite au moins une immunoglobuline sécrétoire est sous une forme inactivée en l'absence d'une quantité réactivatrice de calcium.
  8. Kit de test pour la détection in vitro de la croissance de cellules sensibles aux hormones stéroïdes réversible par des hormones stéroïdes comprenant:
    une population de cellules cancéreuses sensibles aux hormones stéroïdes cultivées qui sont aussi sensibles aux hormones stéroïdes pour une prolifération in vivo;
    un milieu de culture de cellules nutritives défini sans sérum comprenant un fluide nutritif basal substantiellement dénué de Fe (III) non lié et contenant l'ion calcium;
    un inhibiteur à base d'immunoglobuline choisie dans le groupe constitué de IgA, IgM et IgG.
  9. Kit selon la revendication 8, comprenant en outre:
    au moins un additif de test choisi dans le groupe constitué d'hormones stéroïdes et des agonistes et des antagonistes de celles-ci.
  10. Kit selon la revendication 8 ou 9, dans lequel les cellules cancéreuses sensibles aux hormones stéroïdes sont des cellules tumorales mammaires de rat MTW9/PL2.
  11. Kit selon les revendications 8-10, dans lequel l'inhibiteur à base d'immunoglobuline est fourni dans un plasma sanguin appauvri en hormones stéroïdes ou un sérum sanguin appauvri en hormones stéroïdes tel que préparé dans l'une quelconque des revendications 2-5.
  12. Procédé pour la mesure de la quantité d'inhibiteur réversible par des hormones stéroïdes de la croissance de cellules sensibles aux hormones stéroïdes dans un échantillon de fluide corporel comprenant:
    l'appauvrissement de l'échantillon en hormones stéroïdes;
    l'isolement d'une fraction d'inhibiteur à base d'immunoglobuline à partir de l'échantillon appauvri en hormones stéroïdes; et
    tester ladite fraction d'inhibiteur à base d'immunoglobuline appauvri en hormones stéroïdes sur l'inhibition réversible par des hormones stéroïdes de la croissance de cellules sensibles aux hormones stéroïdes dans une population prédéterminée de cellules cultivées maintenues dans un milieu comprenant un fluide nutritif basal substantiellement dénué de Fe (III) non lié et contenant l'ion calcium dans des conditions de culture favorisant la croissance des cellules où les cellules sont sensibles aux hormones stéroïdes pour une prolifération in vivo lors d'une implantation dans un hôte approprié et une augmentation mesurable de l'inhibition de la croissance des cellules avec une augmentation de la concentration de fraction d'inhibiteur à base d'immunoglobuline, à une concentration définie d'hormone stéroïde dans le milieu, indique la quantité d'inhibiteur dans l'échantillon de fluide corporel.
  13. Procédé selon la revendication 11, dans lequel l'échantillon de fluide corporel est choisi dans le groupe constitué de sérum, de plasma, d'urine, de fluide séminal, de lait, de colostrum et de mucus.
  14. Modèle de culture de cellules in vitro pour prévoir un effet d'un stimulus défini sur la croissance de cellules cancéreuses sensibles aux hormones stéroïdes in vivo, comprenant: des cellules cancéreuses sensibles aux hormones stéroïdes maintenues dans un milieu comprenant un fluide nutritif basal substantiellement dénué de Fe (III) non lié et contenant l'ion calcium et contenant une quantité d'inhibiteur à base d'immunoglobuline réversible par des hormones stéroïdes choisie dans le groupe constitué de IgA, IgM et IgG suffisante pour arrêter la croissance de cellules cancéreuses en l'absence d'une quantité inversant l'inhibition d'hormone stéroïde.
  15. Modèle in vitro selon la revendication 13, dans lequel les cellules de culture sensibles aux hormones stéroïdes sont choisies dans le groupe constitué de MTW9/PL2 (cancer mammaire de rat), T47D (carcinome du sein humain), MCF-7 (carcinome du sein humain), MCF-7A (carcinome du sein humain), MCF-7K (carcinome du sein humain), LNCaP (carcinome prostatique humain), ZR-75-I (carcinome prostatique humain), H-30I (tumeur du rein de hamster syrien), GHI et GH3 (tumeur pituitaire de rat), GH4C1 (tumeur pituitaire de rat) et HT-29 (cancer du côlon humain).
EP10184646.7A 2000-05-10 2001-05-10 Compositions et procédés pour le diagnostic, le traitement et la prévention des cancers répondant à l'hormone de croissance Expired - Lifetime EP2394659B1 (fr)

Applications Claiming Priority (6)

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US20331400P 2000-05-10 2000-05-10
US20834800P 2000-05-31 2000-05-31
US20811100P 2000-05-31 2000-05-31
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DE60143320D1 (de) 2010-12-02
EP1366366A2 (fr) 2003-12-03
ATE545433T1 (de) 2012-03-15
US20020012954A1 (en) 2002-01-31
EP2359857A2 (fr) 2011-08-24
EP1328293A2 (fr) 2003-07-23
CA2409150A1 (fr) 2001-11-15
US7947463B2 (en) 2011-05-24
MXPA02011092A (es) 2004-08-19
EP1328293B1 (fr) 2012-02-15
ATE485520T1 (de) 2010-11-15
MXPA02011093A (es) 2004-08-19
CA2409765A1 (fr) 2001-11-15
WO2001086307A2 (fr) 2001-11-15
EP1366366B1 (fr) 2010-10-20
AU2001272908A1 (en) 2001-11-20
EP2394660A1 (fr) 2011-12-14
WO2001085210A3 (fr) 2003-04-17
US20120115161A1 (en) 2012-05-10
US8563249B2 (en) 2013-10-22
EP2359857A3 (fr) 2012-02-22
AU2001269690A1 (en) 2001-11-20
WO2001086307A3 (fr) 2003-10-02
US7947275B2 (en) 2011-05-24
US20020006630A1 (en) 2002-01-17
EP2394659A1 (fr) 2011-12-14
WO2001085210A2 (fr) 2001-11-15

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